Synthesis via vinyl sulfones. 27. Total synthesis of cephalotaxine. The first example of an intramolecular [4 + 2] cycloaddition where the dienophile has been delivered from the face opposite to the tethering moiety

Saved in:
Bibliographic Details
Published in:Journal of the American Chemical Society 1988-03, Vol.110 (7), p.2341-2342
Main Authors: Burkholder, T. P, Fuchs, P. L
Format: Article
Language:English
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-a2144-1a8bf3a7d2a7ba48e57b5ff6504e1a8fcc39bbdd4775e17e3c6e8efe313f14563
cites
container_end_page 2342
container_issue 7
container_start_page 2341
container_title Journal of the American Chemical Society
container_volume 110
creator Burkholder, T. P
Fuchs, P. L
description
doi_str_mv 10.1021/ja00215a076
format article
fullrecord <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_ja00215a076</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>b39812558</sourcerecordid><originalsourceid>FETCH-LOGICAL-a2144-1a8bf3a7d2a7ba48e57b5ff6504e1a8fcc39bbdd4775e17e3c6e8efe313f14563</originalsourceid><addsrcrecordid>eNptkcFu1DAQhiMEEkvhxAvMjUOVbZzEcThCgVJpEUi7cAChaOKMiRfHjmxv2Twpr4PbRRUHDvZo_vnmH40my56zYs2Kkl3ssUiBYyGaB9mK8bLIOSubh9mqSIVctE31OHsSwj6lddmyVfZ7u9g4UtABbjSmZxcD4WCUsxTWUIo17FzEpN1zToGkeUST9KO2lIiRQGkfItARp9nQLYMWtI0eJ2dIHgx6-FbDOZTfQS7SOBwGHbWz8GskT5C8YdBk3Tzq1D9igJ7IwkBG3yRgAOXddIcplGnAPLugY2p0d2Kk9Httf8DkNMXlafZIoQn07G88yz6_e7u7fJ9vPl5dX77a5Fiyus4Ztr2qUAwlih7rlrjouVINL2pKNSVl9bLvh6EWghMTVMmGWlJUsUqxmjfVWXZ-8pXeheBJdbPXE_qlY0V3e5Pun5skOj_ROkQ63qPof3aNqATvdp-23dcPXzZXb15vuzbxL048ytDt3cHbtMt_nf8AuBmfzw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis via vinyl sulfones. 27. Total synthesis of cephalotaxine. The first example of an intramolecular [4 + 2] cycloaddition where the dienophile has been delivered from the face opposite to the tethering moiety</title><source>ACS CRKN Legacy Archives</source><creator>Burkholder, T. P ; Fuchs, P. L</creator><creatorcontrib>Burkholder, T. P ; Fuchs, P. L</creatorcontrib><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/ja00215a076</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of the American Chemical Society, 1988-03, Vol.110 (7), p.2341-2342</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a2144-1a8bf3a7d2a7ba48e57b5ff6504e1a8fcc39bbdd4775e17e3c6e8efe313f14563</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ja00215a076$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ja00215a076$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,27064,27924,27925,56766,56816</link.rule.ids></links><search><creatorcontrib>Burkholder, T. P</creatorcontrib><creatorcontrib>Fuchs, P. L</creatorcontrib><title>Synthesis via vinyl sulfones. 27. Total synthesis of cephalotaxine. The first example of an intramolecular [4 + 2] cycloaddition where the dienophile has been delivered from the face opposite to the tethering moiety</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNptkcFu1DAQhiMEEkvhxAvMjUOVbZzEcThCgVJpEUi7cAChaOKMiRfHjmxv2Twpr4PbRRUHDvZo_vnmH40my56zYs2Kkl3ssUiBYyGaB9mK8bLIOSubh9mqSIVctE31OHsSwj6lddmyVfZ7u9g4UtABbjSmZxcD4WCUsxTWUIo17FzEpN1zToGkeUST9KO2lIiRQGkfItARp9nQLYMWtI0eJ2dIHgx6-FbDOZTfQS7SOBwGHbWz8GskT5C8YdBk3Tzq1D9igJ7IwkBG3yRgAOXddIcplGnAPLugY2p0d2Kk9Httf8DkNMXlafZIoQn07G88yz6_e7u7fJ9vPl5dX77a5Fiyus4Ztr2qUAwlih7rlrjouVINL2pKNSVl9bLvh6EWghMTVMmGWlJUsUqxmjfVWXZ-8pXeheBJdbPXE_qlY0V3e5Pun5skOj_ROkQ63qPof3aNqATvdp-23dcPXzZXb15vuzbxL048ytDt3cHbtMt_nf8AuBmfzw</recordid><startdate>19880301</startdate><enddate>19880301</enddate><creator>Burkholder, T. P</creator><creator>Fuchs, P. L</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19880301</creationdate><title>Synthesis via vinyl sulfones. 27. Total synthesis of cephalotaxine. The first example of an intramolecular [4 + 2] cycloaddition where the dienophile has been delivered from the face opposite to the tethering moiety</title><author>Burkholder, T. P ; Fuchs, P. L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a2144-1a8bf3a7d2a7ba48e57b5ff6504e1a8fcc39bbdd4775e17e3c6e8efe313f14563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Burkholder, T. P</creatorcontrib><creatorcontrib>Fuchs, P. L</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Burkholder, T. P</au><au>Fuchs, P. L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis via vinyl sulfones. 27. Total synthesis of cephalotaxine. The first example of an intramolecular [4 + 2] cycloaddition where the dienophile has been delivered from the face opposite to the tethering moiety</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>1988-03-01</date><risdate>1988</risdate><volume>110</volume><issue>7</issue><spage>2341</spage><epage>2342</epage><pages>2341-2342</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><pub>American Chemical Society</pub><doi>10.1021/ja00215a076</doi><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0002-7863
ispartof Journal of the American Chemical Society, 1988-03, Vol.110 (7), p.2341-2342
issn 0002-7863
1520-5126
language eng
recordid cdi_crossref_primary_10_1021_ja00215a076
source ACS CRKN Legacy Archives
title Synthesis via vinyl sulfones. 27. Total synthesis of cephalotaxine. The first example of an intramolecular [4 + 2] cycloaddition where the dienophile has been delivered from the face opposite to the tethering moiety
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T01%3A41%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20via%20vinyl%20sulfones.%2027.%20Total%20synthesis%20of%20cephalotaxine.%20The%20first%20example%20of%20an%20intramolecular%20%5B4%20+%202%5D%20cycloaddition%20where%20the%20dienophile%20has%20been%20delivered%20from%20the%20face%20opposite%20to%20the%20tethering%20moiety&rft.jtitle=Journal%20of%20the%20American%20Chemical%20Society&rft.au=Burkholder,%20T.%20P&rft.date=1988-03-01&rft.volume=110&rft.issue=7&rft.spage=2341&rft.epage=2342&rft.pages=2341-2342&rft.issn=0002-7863&rft.eissn=1520-5126&rft_id=info:doi/10.1021/ja00215a076&rft_dat=%3Cacs_cross%3Eb39812558%3C/acs_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a2144-1a8bf3a7d2a7ba48e57b5ff6504e1a8fcc39bbdd4775e17e3c6e8efe313f14563%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true